Literature DB >> 10719897

Analysis of clock proteins in mouse SCN demonstrates phylogenetic divergence of the circadian clockwork and resetting mechanisms.

M D Field1, E S Maywood, J A O'Brien, D R Weaver, S M Reppert, M H Hastings.   

Abstract

The circadian clock in the suprachiasmatic nuclei (SCN) is comprised of a cell-autonomous, autoregulatory transcriptional/translational feedback loop. Its molecular components include three period and two cryptochrome genes. We describe circadian patterns of expression of mPER2 and mPER3 in the mouse SCN that are synchronous to those for mPER1, mCRY1, and mCRY2. Coimmunoprecipitation experiments demonstrate in vivo associations of the SCN mPER proteins with each other and with the mCRY proteins, and of mCRY proteins with mTIM, but no mPER/mTIM interactions. Examination of the effects of weak and strong resetting light pulses on SCN clock proteins highlights a central role for mPER1 in photic entrainment, with no acute light effects on either the mCRY or mTIM proteins. These clock protein interactions and photic responses in mice are divergent from those described in Drosophila.

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Year:  2000        PMID: 10719897     DOI: 10.1016/s0896-6273(00)80906-x

Source DB:  PubMed          Journal:  Neuron        ISSN: 0896-6273            Impact factor:   17.173


  101 in total

1.  Coiled-coil domain-mediated FRQ-FRQ interaction is essential for its circadian clock function in Neurospora.

Authors:  P Cheng; Y Yang; C Heintzen; Y Liu
Journal:  EMBO J       Date:  2001-01-15       Impact factor: 11.598

2.  Nucleocytoplasmic shuttling and mCRY-dependent inhibition of ubiquitylation of the mPER2 clock protein.

Authors:  Kazuhiro Yagita; Filippo Tamanini; Maya Yasuda; Jan H J Hoeijmakers; Gijsbertus T J van der Horst; Hitoshi Okamura
Journal:  EMBO J       Date:  2002-03-15       Impact factor: 11.598

3.  Dissociation between light-induced phase shift of the circadian rhythm and clock gene expression in mice lacking the pituitary adenylate cyclase activating polypeptide type 1 receptor.

Authors:  J Hannibal; F Jamen; H S Nielsen; L Journot; P Brabet; J Fahrenkrug
Journal:  J Neurosci       Date:  2001-07-01       Impact factor: 6.167

4.  Nuclear export of mammalian PERIOD proteins.

Authors:  E L Vielhaber; D Duricka; K S Ullman; D M Virshup
Journal:  J Biol Chem       Date:  2001-10-08       Impact factor: 5.157

5.  Dimerization and nuclear entry of mPER proteins in mammalian cells.

Authors:  K Yagita; S Yamaguchi; F Tamanini; G T van Der Horst; J H Hoeijmakers; A Yasui; J J Loros; J C Dunlap; H Okamura
Journal:  Genes Dev       Date:  2000-06-01       Impact factor: 11.361

6.  Light and glutamate-induced degradation of the circadian oscillating protein BMAL1 during the mammalian clock resetting.

Authors:  T Tamaru; Y Isojima; T Yamada; M Okada; K Nagai; K Takamatsu
Journal:  J Neurosci       Date:  2000-10-15       Impact factor: 6.167

7.  Targeted disruption of the mPer3 gene: subtle effects on circadian clock function.

Authors:  L P Shearman; X Jin; C Lee; S M Reppert; D R Weaver
Journal:  Mol Cell Biol       Date:  2000-09       Impact factor: 4.272

8.  Light-regulated translation mediates gated induction of the Arabidopsis clock protein LHY.

Authors:  Jae-Yean Kim; Hae-Ryong Song; Bethan L Taylor; Isabelle A Carré
Journal:  EMBO J       Date:  2003-02-17       Impact factor: 11.598

9.  Of switches and hourglasses: regulation of subcellular traffic in circadian clocks by phosphorylation.

Authors:  Ozgür Tataroğlu; Tobias Schafmeier
Journal:  EMBO Rep       Date:  2010-11-05       Impact factor: 8.807

10.  Expression profiles of PER2 immunoreactivity within the shell and core regions of the rat suprachiasmatic nucleus: lack of effect of photic entrainment and disruption by constant light.

Authors:  Christian Beaulé; Lisa M Houle; Shimon Amir
Journal:  J Mol Neurosci       Date:  2003       Impact factor: 3.444

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